IWEPoissonPaper

IWEPoissonPaper models CpG island-wide DNA methylation dynamics in vertebrate genomes to capture interdependent methylation changes across clustered CpG sites and to infer branch lengths in cell type phylogenies.


Key Features:

  • Probabilistic Modeling: Captures simultaneous methylation changes across multiple CpG sites within the same CpG island by modeling interdependence of methylation states.
  • Markov-Chain Monte-Carlo (MCMC) Methodology: Employs MCMC to fit the probabilistic model to methylation data derived from cell type phylogenies.
  • Inference of Phylogenetic Branch Lengths: Infers branch lengths in cell phylogenies based on methylation changes.
  • Application to Murine Haematopoietic Cells: Has been applied to methylation data from murine haematopoietic cells to capture developmental methylation pattern changes.

Scientific Applications:

  • Gene Regulation Studies: Supports analysis of how CpG island-wide methylation dynamics influence gene expression across cell types.
  • Developmental Biology: Provides inference of lineage divergence and developmental processes via methylation-based branch length estimates.
  • Epigenetics Research: Offers a framework for studying complex methylation patterns within CpG islands and their effects on cellular function and organismal development.
  • Murine Haematopoiesis Analysis: Demonstrated utility on murine haematopoietic cell methylation datasets to study differentiation-associated methylation changes.

Methodology:

Integrates CpG island-wide probabilistic models of methylation dynamics and fits them to methylation data from cell type phylogenies using Markov-Chain Monte-Carlo (MCMC) inference.

Topics

Details

License:
GPL-3.0
Maturity:
Mature
Cost:
Free of charge
Tool Type:
command-line tool
Operating Systems:
Linux, Windows, Mac
Programming Languages:
C++
Added:
8/9/2019
Last Updated:
6/16/2020

Operations

Publications

Grosser K, Metzler D. Modeling methylation dynamics with simultaneous changes in CpG islands. Unknown Journal. 2019. doi:10.1101/638023.

Links